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Our Core Laboratory Instrumentation

Our laboratory combines cutting-edge technology with expert methodologies to deliver analytical solutions for every stage of your CMC journey. Have a specific analytical need? Reach out, and we'll provide the expertise and support your project requires.

Have a specific analytical need? Reach out, and we'll provide the expertise and support your project requires.

Gas Chromatography (GC) instrument for volatile compound analysis in pharmaceutical development.

  • 16 Analytical HPLC/UPLC instruments (Agilent 1100, 1200, 1260, 1290 and Waters Acquity)​

  • ​UV/DAD, ELSD, CAD, FLD detectors

  • 2 LC/MSD (single quadrupole)

  • 1 LC/MSD (Q-TOF Agilent 6540)

  • 1 Preparative HPLC (Agilent 1260 with VWD)

  • Gas Chromatograph with FID (direct injection) Agilent 6890

  • Gas Chromatograph with FID and Headspace Agilent 8890

  • 5 Dissolution Instruments (USP Apparatus 1 & 2)

  • Disintegration apparatus

  • UV/VIS spectrophotometer (Agilent 8453)

  • Solo VPE Agilent Cary 60 UV-VIS Spectrophotometer

  • Agilent G1600AX Capillary Electrophoresis

  • FTIR spectrometer (Perkin Elmer Spectrum 2)

  • Karl Fischer Titrator with oven (Metrohm 852 Titrando)

  • Malvern Mastersizer 3000

USP dissolution testing apparatus for evaluating drug release rates in formulation development and quality control.
Temperature-controlled stability chamber for long-term drug stability testing under ICH guidelines.

  • DSC Q2000 TA Instruments

  • TGA Q500 TA Instruments

  • Photostability Chamber (ICH) - Caron

  • ICH Stability Chambers:​

  • 5°C, 25°C/60%RH, 30°C/65%RH, 40°C/75%RH​

  • Refrigerators & Freezers

  • Variable temperature/humidity-controlled ovens

  • Innova temperature-controlled incubator-shaker

  • Centrifuges (including temperature-controlled)

  • Milli-Q in-house water

  • pH meters, ultrasonic baths, stirring plates

  • Through Partnership:

  • NMR

  • XRPD

  • Microbial testing

EZ Labs provides reliable impurity profiling and degradation analysis.
Our GMP-compliant analytical lab combines expertise, precision, and innovation to solve your toughest analytical challenges.

  • 16 Analytical HPLC instruments (Agilent 1100, 1200, 1260, 1290, and Waters Acquity)​

  • ​UV/DAD, ELSD, CAD, FLD detectors

  • Gas Chromatograph with FID and Headspace Agilent 8890

  • ICH Stability Chambers:​

  • 5°C, 25°C/60%RH, 30°C/65%RH, 40°C/75%RH​

  • Refrigerators & Freezers

  • Photostability Chamber (ICH) - Caron

  • Variable temperature/humidity-controlled ovens

  • Innova temperature-controlled incubator-shaker

  • 5 Dissolution Instruments (USP Apparatus 1 & 2)

  • Disintegration apparatus

  • UV/VIS spectrophotometer (Agilent 8453)

  • 1 Preparative HPLC (Agilent 1260 with VWD)

  • Karl Fischer Titrator with oven (Metrohm 852 Titrando)

  • Malvern Mastersizer 3000

  • DSC Q2000 TA Instruments

  • TGA Q500 TA Instruments

  • Solo VPE Agilent Cary 60 UV-VIS Spectrophotometer

  • Agilent G1600AX Capillary Electrophoresis

  • FTIR spectrometer (Perkin Elmer Spectrum 2)

  • 2 LC/MSD (single quadrupole)

  • 1 LC/MSD (Q-TOF Agilent 6540)

  • Gas Chromatograph with FID (direct injection) Agilent 6890

Through Partnership:

  • NMR

  • XRPD

  • Microbial testing

  • Centrifuges (including temperature-controlled)

  • Milli-Q in-house water

  • pH meters, ultrasonic baths, stirring plates

Contact EZ Labs Today

to discuss how we can best support your project

High-Performance Liquid Chromatography (HPLC) system for precise compound separation in CMC analytical testing.

  • Development, qualification, validation, and transfer of HPLC/GC assay and impurities methods

  • Forced degradation studies including ID of the degradation products

  • Providing analytical and stability data for regulatory submissions (Module 3)

  • Development and validation of methods for PGIs at the ppm levels per ICH M7

  • Chiral HPLC method development and validation

  • Impurities identification, structure elucidation

  • Formulation development support: Tox formulations, stability, excipient compatibility, solubility

  • Development of dissolution methods including NDA level discriminating methods

  • Dissolution testing in biorelevant and QC media in support of DOE and regulatory submissions

  • GMP release testing and ICH stability studies for DS and DP Phase 1-2 clinical programs

  • Reference standards characterization and management

  • Reference standards characterization and management

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